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  1. Plasmids 101: Sequence and Ligation Independent Cloning (SLIC)

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    Blog Post
    ...restriction enzyme cloning uses short sticky ends to insert genes into plasmid backbones, base pairing between...absence of the other dNTPs. Once the vector and insert are (separately) digested to create 10–12 base ...on the power of homologous recombination. SLIC inserts and linearized vectors must have homologous DNA...imprecise T4 digestion (no dNTPs needed), allows both insert and vector to be digested in the same tube. Alternatively...these approaches require higher concentrations of insert to succeed. 5′ overhangs are generated in the linearized... be used with different types of PCR-generated inserts. By harnessing the power of DNA repair, you can...
  2. Viral Vectors 101: Viral Vector Elements

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    ...interact with the host. This is the role of Gag proteins: they contain the matrix, capsid, and nucleocapsid...assembly, and display. Pol, the last component, contains the reverse transcriptase and integrase components...convert the cargo from RNA to DNA and permanently insert the cargo into the host genome. Lentiviral-specific... Viral packaging and entry The viral packaging proteins for AAV are rep and cap. Rep is required for viral...discussed. LXs/Iva2 are primarily capsid assembly proteins required for packaging of the virus into particles...Resources Kulanayake, S., Tikoo, S. K. Adenovirus Core Proteins: Structure and Function. Viruses. 2021 13(3):388...
  3. Viral Vectors 101: Types of viruses

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    Blog Post
    ...proto-oncogenes and disrupt their expression (Robinson, 1982). To add insult to injury, retroviruses generally have...This viral DNA (also called proviral DNA) is then inserted into the host's genome and is used to make more...virus-specific elements such as the LTRs or structural proteins are not interchangeable between the two systems...Adenovirus generally has high immunogenicity, but some strains have been engineered to induce a lower inflammatory...immunogenicity low! References and Resources References Robinson HL. Retroviruses and cancer. Rev Infect Dis. 1982...
  4. Enabling Precision Functional Genomics with the Target Accelerator Plasmid Collection

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    ...Associate Director of the Cancer Program at the Broad Institute of Harvard and MIT. The notion of cancer precision...We've developed a new plasmid toolkit, the Broad Institute Target Accelerator Plasmid Collection, that we...variant function and cancer phenotypes. Broad Institute Target Accelerator Plasmid Collections To overcome...this first challenge, we’ve developed the Broad Institute Target Accelerator Plasmid Collections, now widely...Associate Director of the Cancer Program at the Broad Institute of Harvard and MIT and is focused on making precision...Kits at Addgene Browse Plasmids from the Broad Institute ...
  5. Addgene’s Viral Service - Why Virus? Why Now?

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    ...Root from the Broad Institute and Alex Chavez from the Wyss Institute were instrumental in helping us establish...School, and Jonathan Ting’s lab from the Allen Institute have supported the AAV initiative from the beginning...Janelia Research Campus have provided valuable insight into AAV production. Finally, we are blessed to...permission from relevant plasmid depositors and their institutions to distribute viral preps derived from plasmids...
  6. Plasmids 101: Methylation and Restriction Enzymes

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    ...if not methylated (if it comes from a phage for instance). Aside from restriction modification systems,...effectively cleave DNA. Common lab E. coli K12 strains such as DH5alpha contain 3 methylases that recognize...Dam or Dcm methylation, you can ensure this site remains unblocked by first cloning your DNA into a dam–...and re-purifying it. These specialized E. coli strains have been specifically engineered to be Dam and...those sites. Please keep in mind that dam-/dcm- strains may have an increased rate of mutation (as these...in mis-match repair functions of Dam), so these strains should not be used for long term storage. Additional...
  7. How to Keep a Lab Notebook for Bioinformatic Analyses

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    Blog Post
    ...another name for a folder. For instance, your Desktop directory contains the folders and files that you...including background on other analyses that have inspired you to perform this analysis. Having a clearly...multiple projects in a given day. For example, instead of naming a file “output” name the file “1_output...subsequent word in a file name after the first word begins with a capital letter and words are not separated...temporarily used. Just be sure that the original code remains in tact! Take notes Comment in your scripts: ...
  8. Protein Tagging with CRISPR/Cas9: A Conversation with Mendenhall and Myers

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    ...small percentage of the proteins inside a cell have a commercial antibody against them. There’s also a question...Mendenhall of the University of Alabama in Huntsville explains it, a major goal in his laboratory is to understand...track down every last one of those gene regulatory proteins and the places in the genome where they can be.... If things work correctly, the second plasmid inserts a small epitope tag called FLAG at the end of the...
  9. Pooled CRISPR Libraries Offer Genome-Wide Control for Large-Scale Functional Screens

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    ...and control genes, but according to the Broad Institute's Silvana Konermann, the first generation of CRISPR-Cas9...recognized as an ideal spot to fuse the activators instead of at the protein’s C terminus. With that new design... and knew she was on the right track. The next insight was to assemble a synthetic transcription activation...complex consisting of multiple distinct effector domains that work together synergistically, modeled after...CRISPRa) sgRNA library uses the sunCas9 system and contains 10 sgRNAs for each transcription start site in...The transcriptional repressor (CRISPRi) library contains 10 sgRNAs for each transcription start site in...
  10. Plasmids 101: Yeast Vectors

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    ...occurring resistant mutants and the insensitivity of yeast strains to some antibiotics. Auxotrophy is ...bacteria, yeast can post-translationally modify proteins yet they still share many of the same technical...replication (Please note: This first section primarily pertains to ORIs in budding yeast, Saccharomyces cerevisiae...other hand, do not require a well defined ORI. Instead, the size and A-T content of the DNA (apparently...compound required for its growth. Many auxotrophic strains of yeast exist which can be easily maintained when...
  11. Plasmids 101: Modular Cloning Applications and Kits

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    ...multiplexing of sgRNAs against unique genomic targets or multiple sgRNAs against the same target to ensure...protein purification and metabolic engineering. If instead you want to build genetic circuits and would benefit...library of parts but don’t need to add tags to your proteins, then the CIDAR Kit is an excellent option (Iverson...system includes a toolkit to express recombinant proteins within the mitochondrial matrix.     Figure...can be repurposed for CRISPR applications (gene insert = Cas9 + gRNA), Addgene distributes specialized...of a Toolkit for the Expression of Heterologous Proteins in Yeast Mitochondria.” BMC Biotechnology, vol...
  12. What's New in CRISPR - November 2021

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    ...genomic deletions with or without small insertions. But, instead, PEDAR couples this deletion process to...mammalian cells, especially when fused to effector proteins for gene activation or gene editing. The more ... lab adapted the native PEG10 RNA sequences to instead drive packaging of cargo sequences in the capsid...it is also capable of coding concurrent small insertions to allow in-frame deletions and introduce epitope...mouse model of tyrosinemia, where a pathogenic insertion within the FAH gene was precisely corrected, restoring...
  13. Supporting Rare Disease Research with the 2020 BeHEARD Awards

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    ...The Rare Genomics Institute BeHEARD (Helping Empower and Accelerate Research Discoveries) Challenge provides...our fourth year working with the Rare Genomics Institute by providing plasmid-based tools for rare disease...Addgene to set up assays to see what molecules or proteins are involved in IL-36 release in keratinocytes... valve (an aortic valve that has two leaflets, instead of three) and acute aortic dissections (a tear ...standing interest in the biology of GPCRs and G proteins, with an emphasis on oligomerization, signalling...Resources Find out more about the Rare Genomics Institute and this year's BeHeard Award! ...
  14. Troubleshooting Your Plasmid Cloning Experiment

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    ...plasmid is the correct expected size and contains the correct insert Sequence the regions that have been amplified...DNA. As a general rule, try to use an excess of insert compared to the backbone plasmid; a starting point...point could be a molar ratio of 1:2 (plasmid:insert), but this parameter has to be optimized according...transforming the ligation mix in different bacterial strains (stbl2, NEB stable, etc.), and/or use a different...primers. If not, design primers to sequence your insert. When you get your sequencing results back, you...
  15. Hot Plasmids April 2018 - Protein Degradation, Nanoscopy, FIRE-Cas9, and Yeast Expression Tools

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    ... ZIF268 DNA binding domains fused to either the hER or hPR ligand binding domains and the MSN2 transactivation...Schuh labs. Clift et al. applied TRIM-away to nine proteins in ten ddifferent cell types, including difficult-to-manipulate...TRIM-Away is suitable for both short-and long-lived proteins, and it can even distinguish between protein variants... STED nanoscopy Article contributed by Eric J. Perkins Listen to Endosomal pH Sensors podcast segment ...plasmids encoding fluorescent reporters and other proteins controlled by GAL4 and ZIF268. To demonstrate ...
  16. Developing Lab Management Software for Biology

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    ... learned over the years with the hope that our insights can help steer you in the right direction when... in our current setup, there are no explicit instructions on what to do when something fails. While we... through which she could easily transfer her instructions for dealing with the samples to newer lab members... ourselves up for success by giving explicit instructions to lab members through the software if there...collisions you may encounter: vector, sequence, insert, trait, factor, expression, etc.There are also ...biology terms (plasmid, 5-prime, CRISPR, growth strains, vector backbone, etc.) and you simply don't have...
  17. CRISPR Meets Synthetic Biology: A Conversation with MIT’s Christopher Voigt

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    ...As Christopher Voigt explains it, his lab at the Massachusetts Institute of Technology has been “working...create an almost limitless number of DNA binding proteins with Cas9 guided by different promoters. The challenge... genetic circuits is getting enough regulatory proteins that don’t interfere with each other. CRISPR is...much easier it is to work with than regulatory proteins. There are still things we haven’t solved that...Nothing too much more sophisticated. There are also proteins, like antibodies. But we are really just using...
  18. Working with Nuclear Receptors

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    ...controlled by deliberate and compulsory actions instigated by the central nervous system signaling to peripheral...sensors for a diverse set of fat-soluble hormones, vitamins, and dietary lipids. Included in this family are...progesterone, androgens, and estrogens), fat-soluble vitamins A and D, thyroid hormone, fatty acids, oxysterols...composed of a tightly-bound invariant group of proteins, whereas the more loosely bound co-coregulators...explain how more than 300 different coactivator proteins individually contribute to cell regulation in ...acetyltransferase to luciferase, the basic assay remains widely used today.  The sheer abundance of these...
  19. Progress Towards a PAM-Free CRISPR

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    ...or non-existent PAM requirement, and how these proteins are advantageous in today’s genome editing landscape...the site in question (Kwart et al, 2017). To add insult to injury, the most utilized PAM sequence, that...requirements. Luckily, there are some available.   Cas proteins that don’t utilize NGG   There are plenty of Cas9...same PAM preference of NG was isolated by the Kleinstiver Lab (read more on this lab's other developments...developments below!) (Walton et. al, 2020). These Cas proteins have everything we know and love about Cas9, but...and location.   Nearly PAM-less editing   The Kleinstiver lab sought to address the PAM problem through...
  20. Degrading DNA with Cascade-Cas3

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    ..., and Cas11. Type I-E Cascades contains all five of these Cas proteins, while type I-C Cascades do not...boundaries defined by anti-CRISPR proteins or running into other proteins naturally bound to the DNA. Cas3...The helicase domain is then activated, and Cas3 begins unraveling the double-stranded DNA (dsDNA) in what...Cas9 vs. The Other Cas(s) CRISPR 101: Anti-CRISPR Proteins Switch Off CRISPR-Cas Systems INTEGRATE: Bacterial...
  21. Common Injection Routes in Mice

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    ... as “instillation” or “gavage,” as they do not require any punctures. Intratracheal instillation Intratracheal...Skill required: advanced Intranasal instillation Intranasal instillation is very similar to its intratracheal...compounds, as circulation is slower, and more institutional oversight is required. Restraint: mechanical...Intratracheal instillation is used to deliver substances directly to the lungs. It is an advanced technique...
  22. Antibodies 101: Flow Compensation

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    ... depending on your flow cytometer’s setup. For instance, BV510 and AmCyan have almost identical emission...and how do I fix it? When plotting two channels against each other, you should be able to draw perpendicular...single-color APC control, with APC and APC-CY7 plotted against each other. Since it is a single-color control,...After increasing the compensation values for APC against APC-Cy7, the populations are in more of a straight...compensation value of five was applied to APC-Cy7 against APC to correct for this bleed. A compensation value...population is not a double-positive population and is instead due to bleeding, you will see the populations move...
  23. Adenoviral Delivery of CRISPR/Cas9 Aims to Expand Genome Editing to Primary Cells

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    ...encapsulating the genome is majorly composed of three proteins that can be easily modified in order to facilitate...provide a large transgene packaging capacity. For instance, with a packaging capacity of about 6 kb, the ...mechanism to knock out genes as a result of an insertion, a deletion or a frameshift (Ding et al., 2014...attribute this phenomenon to the presence of terminal proteins capping the ends of linear double-stranded AdV...several biological systems. It has been used for instance in inherited disorders such as B-thalassemia, ...steatohepatitis cancer. In deficiencies of plasma proteins where Adv vector delivery is often used, the CRISPR...
  24. Mobile-CRISPRi: Bringing CRISPRi to Diverse Bacteria

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    ...resistance selection markers, gRNAs, and dCas9 proteins. Second, it can be introduced into a broader range...tnsB, tnsC, tnsD, and tnsE), and a plasmid that contains the Mobile CRISPRi cassette flanked by left and...recipient's genome. Antibiotic plates lacking DAP select against donor bacteria and for recipients with an integrated...CRISPRi to non-model bacteria including pathogenic strains and environmental isolates. For example, Peters...expressed RFP reporter, was variable across bacterial strains, ranging from an ~8 to 150-fold reduction, with...the relative frequency of each of the 40 library strains was measured after 6 and 12 generations with or...
  25. Tips for a 1st time AAV user (by a Rookie AAV user)

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    ... myself writing AAV production tricks into the margins of my protocol. While these tips weren’t critical...replication uses the host’s polymerase, but requires Rep proteins to process a double-stranded intermediate into...cultures of your AAV transfer plasmid at 30 °C instead of 37 °C and then screen for ITR recombination ...transform AAV transfer plasmids into bacterial strains, like NEB Stable. NEB Stable competent cells lack... should consider performing PEG precipitation. Instead of sonicating the cell pellet, I lyse the cells... Stone and Harshana de Silva Feelixge at Fred Hutchinson Cancer Center for teaching me about AAV production...
  26. Transgenic Organisms, Cas9 Gene Drives, and Appropriate Safeguards

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    ...Wyss Technology Development Fellow at the Wyss Institute and Harvard Medical School. Scientists making ...drive? The simplest way to make a gene drive is to insert an endonuclease gene within its own cut site1. ...spreads through the wild population and immunizes it against the first drive. Laboratories interested in building...question), why not use them whenever applicable?Against this, consider the cost of an accidental release...accidental release could delay real-world applications against scourges such as malaria and dengue for many years... Holm, D. G. & Suzuki, D. T. Genetic Control of Insect Populations: I. Cage Studies of Chromosome Replacement...
  27. DNA Purification Without a Kit

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    ...causes the proteins and genomic DNA to precipitate. Plasmid DNA is free in solution. Proteins and genomic...the same principles: cells are lysed, RNAs and proteins are removed to leave you with DNA. This DNA is...you lyse the bacteria and denature the DNA and proteins in solution. The pH is then lowered using a renaturing...phenol chloroform extraction to remove remaining proteins and RNase. Finally, DNA is precipitated with alcohol...identical to that of commercially available kits but instead of binding DNA to silica columns, it’s bound to...
  28. CRISPR 101: Ribonucleoprotein (RNP) Delivery

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    ...such as PX459, which encodes Cas9 and contains a site for inserting a custom gRNA.  While this methodology...translation delays editing What are Cas9-gRNA ribonucleoproteins? One alternative approach, which avoids many...Schier laboratories. Delivering Cas9-gRNA ribonucleoproteins  An advantage of performing CRISPR experiments...vivo applications. This technique utilizes Cas9 proteins harboring receptor ligands (C in the figure above...., et al. "Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing...
  29. Tips and Tricks for Using Golden Gate Modular Cloning (MoClo)

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    ...terminator. Created with BioRender.com. The Sainsbury Laboratory Golden Gate Cloning videos made by ...according to their concentration, size, and the desired insert-to-vector ratio using the equation in Figure 3....plasmid volume for MoClo experiments. The term ‘insert’ refers to plasmids carrying each part, ‘vector... the ‘amount of vector’ and the ‘molar ratio of insert to vector’ can be defined by you.   Save time...each transformation and/or use different E. coli strains with higher transformation efficiency. If you’re...We strongly encourage you to sequence the entire insert region of your final plasmid or those you are selecting...
  30. Plasmids 101: Shuttle Vectors

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    ...origin of replication (ori), where DNA replication begins, so a bacterial plasmid needs a compatible ori ... divide. In transient transfection, the vector remains episomal, meaning it stays separate from the genome...synthesis, and the neomycin resistance gene protects against any of them. But different aminoglycosides work...options doesn’t end there. Make sure you read the instructions for whatever antibiotic you choose to ensure...to spontaneously develop resistance to selection toxins. Auxotrophic selection is useful for producing ...researcher may choose not impose selection on cells and instead to use a vector with a reporter, such as a fluorescent...
  31. CRISPR 101: Which Cas9 Do I Choose for My CRISPR Experiment?

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    ...with higher specificity (eSpCas9 and HypaCas9) instead.  Choosing a Cas9 for site-specific modifications... effects. The SpG variant, discovered by the Kleinstiver group has a PAM of NGN (Walton et al., 2020)....system can be used with a variety of impaired Cas9 proteins (such as SpRY) with altered PAM requirements, ...facilitates recruitment of multiple activation domains to the same genetic locus via co-expression of ...epitope tagged dCas9 and antibody-activator fusion proteins. The Synergistic Activation Mediator complex, ..., R. T., Christie, K. A., Whittaker, M. N. & Kleinstiver, B. P. Unconstrained genome targeting with near-PAMless...
  32. Transferable Skills Guide: Creativity

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    ...yourself needing to brainstorm with a team. One major challenge with these brainstorming sessions is avoiding...with unlimited time? Another strategy for your brainstorm session is to start with something completely... students during an interview. When they were instructed to use the three-ring binder as a starting point...people to agree with the most prominent idea, and instead building an environment where everyone has their... ideas that I have found helpful in my team brainstorming sessions.  Allow the group time to think about...
  33. Save Time with Transient Plant Leaf Transformations

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    ...these experiments can be done in days to weeks instead of months to years. In the plant sciences “transient...evaluate its function. In nature Agrobacterium contains a plasmid with a T-DNA (transfer-DNA) region. ...pSB166 - pL2_pSB90_tMAS::rLUC-I::pMAS. Fluorescent proteins (FP, e.g. GFP) can be used in many ways. Often...from Agrobacterium. Test different Agrobacterium strains We used the disarmed Agrobacterium tumefaciens ...plants using syringe agroinfiltration." Recombinant proteins from plants. Humana Press, 2009. 41-50. PubMed... 5.02 (2003): 103-115. Hu, Ching-yeh, et al. "Intrinsic GUS-like activities in seed plants." Plant cell...
  34. Advanced Uses of Cre-lox and Flp-FRT - A Neuroscientist’s View

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    ...expression while proteins needed for later experiments (cellular tracking for instance) can be controlled...Tamoxifen is added. Tamoxifen then binds to the ER-LDB domains of the fusions allowing Cre/FLP translocate to ...fluorescent cytoplasmic markers (e.g. eYFP) and synaptic proteins (e.g. postsynaptic PSD95-mcherry) are used in ...In order to analyze the function of individual proteins in neuronal circuits or synaptic remodeling, researchers...is fascinated by the question of how genes and proteins coordinate billions of neurons to form the functional...
  35. Healthcare Consulting: A Door to the Business of Life Sciences

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    ...pharmaceutical companies, biotech start-ups, health insurance companies, and governments on the most effective...physicians and patients, shaping discussions with insurance companies about the pricing and coverage of drugs...situations might be especially challenging. For instance, the client might need to get a large amount of...occasions, clients can be excessively demanding. For instance, a client may offer a lot of pointed feedback ...understanding of the molecular behaviors of chemicals and proteins to learn how a particular drug or medical device...therapeutic approach brings to patients, doctors, and insurance providers, and is crucial to how our clients’ ...
  36. New Optogenetic Tools for Cytoskeleton and Membrane Control

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    ...to reveal even more insights. Super-duper lipid editor And if recruiting proteins to the cell membrane...photoswitchable elements into many other types of proteins. Here, we’ll highlight a few recently-deposited...et al., 2022). Stopping traffic with CIB1-Rabs Instead of using an optogenetic module to activate or recruit...such a strategy to dissect the roles of three Rab proteins during a key stage of zebrafish development (Aljiboury...(Aljiboury et al., 2023). Rab family proteins support vesicle trafficking and organelle dynamics, but ...
  37. Five Popular Model Organisms, Part 2

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    ..., R., Weinstock, G., Metzker, M. et al. Genome sequence of the Brown Norway rat yields insights into mammalian...organism in microbiology and biochemistry. Certain strains have been specifically developed to thrive in laboratory...extensive research history and characterization. Many proteins and processes naturally found in E. coli have ...amphibians in science with early research providing insight into some of the most significant and fundamental...), 565–571. https://doi.org/10.1159/000323761 Modlinska, K., & Pisula, W. (2020). The Norway rat, from...
  38. The Fluorescent Vegetables in Aptamer Soup

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    ...unstable in vivo due to poor folding and thermal instability at 37°C (Ouellet et al., 2016) and requires a...riboswitch, metabolite binding to the riboswitch instead activates Spinach fluorescence. In the search for...identified the nucleotides that contribute to the instability of Spinach, and were able to develop an aptamer...Spinach, a miniaturized version of Spinach that retains similar levels of fluorescence when bound to DFHBI... cell imaging. Bunch of baby spinach, or BoBS, contains tandem repeats of Baby Spinach. It was developed... Aliyah Weinstein...
  39. Site Directed Mutagenesis by PCR

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    ...reporter constructs), in functional analysis of proteins (to perform alanine scanning mutagenesis or targeted...should be resistant to Cas9 cleavage. If a plasmid contains the template, site-directed mutagenesis can be...which is dam+). Methylation deficient bacterial strains can be identified by the dam13(-) mutation – you...you’ll want to steer clear of these strains when preparing the plasmid template for site directed mutagenesis...functional regions of the plasmid including the insert. This is essential since mutations are potentially...PubMed PMID: 2448875. 4. Xia, Yongzhen, et al. "New insights into the QuikChangeTM process guide the use of...
  40. Evolution of Lab Techniques

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    ...whether you are perusing classic papers or are brainstorming new technological innovations. Let’s take a ...blotting to screen founder transgenic animals for the inserted transgene because Southern blots have a lower ...digests. A researcher can test the orientation of an insert in only a few hours at low cost with restriction...do not typically rely on Sanger sequencing but instead use methods like pyrosequencing that are parallelized...techniques we use now may soon become obsolete. For instance, the popular genome-engineering tool, CRISPR, ...mouse lines, such as BAC transgenic or traditional knockins/knockouts, a thing of the past. In the sequencing...
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